GNG2

protein-coding

G protein subunit gamma 2, the group of G protein subunits gamma

Gene summary

This gene encodes one of the gamma subunits of a guanine nucleotide-binding protein. Such proteins are involved in signaling mechanisms across membranes. Various subunits forms heterodimers which then interact with the different signal molecules. [provided by RefSeq, Aug 2011]

MANE transcript

NM_053064.5

Inheritance

—

ClinVar variants

U:4

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 0

Max pathogenic AF

—

Genomic locus

chr14:51,826,195-51,979,342

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~153.1 kb
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GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to GNG2 variants in ClinVar

1 Conditions Cataloged
not specifiedTotal: 4

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_053064.5. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
4
clinvar
4
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total004004
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 62 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_053064.5RefSeqNP_444292.12MANE Select
ENST00000556766.6EnsemblENSP00000451231.12MANE Select
NM_001243773.2RefSeqNP_001230702.12Standard
NM_001243774.2RefSeqNP_001230703.12Standard

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Pathways ConsensusPathDB

  • PI3K-Akt signaling pathway - Homo sapiens (human)
  • Relaxin signaling pathway - Homo sapiens (human)
  • Kaposi,s sarcoma-associated herpesvirus infection - Homo sapiens (human)
  • Retrograde endocannabinoid signaling - Homo sapiens (human)
  • GABAergic synapse - Homo sapiens (human)

Biological Process

  • protein folding
  • G protein-coupled receptor signaling pathway
  • adenylate cyclase-activating dopamine receptor signaling pathway
  • Wnt signaling pathway, calcium modulating pathway
  • cell population proliferation

Molecular Function

  • GTPase activity
  • protein binding
  • G-protein beta-subunit binding

Cellular Component

  • heterotrimeric G-protein complex
  • plasma membrane
  • membrane
  • extracellular exosome

gnomAD Constraint

Source: gnomAD

Gene type
protein_coding
Transcript type
protein_coding
Transcript
ENST00000335281
Coding exons
2
Length
153148
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense1.281739.70.4280.00000200469
Missense (PolyPhen)515.2740.32735201
Synonymous0.2021516.00.9360.00000102131
Loss of Function1.3101.990.008.31e-827

Population LoF Frequency

PopulationCAFp-valueStatus
African00.0absent
Latino/Admixed American00.0absent
Ashkenazi Jewish00.0absent
East Asian00.0absent
Finnish00.0absent
European (Non-Finnish)00.0absent
South Asian00.0absent
Other00.0absent

dbNSFP Gene Annotations

Source: dbNSFP

Function
FUNCTION: Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein- effector interaction (By similarity). {ECO:0000250}.;

Recessive Scores

pRec
0.142

Intolerance Scores

LoFtool
0.503
RVIS EVS
0.06
RVIS percentile EVS
58

Essentials

Essential (CRISPR)
N
Essential (CRISPR2)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.192

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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